rs146221617 Rat Genome Database

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Variant: rs146221617 -  Homo sapiens

RGD ID: 150412803
RS ID: rs146221617
ClinVar ID: CV1190173
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ETFDH  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 159,616,446
GRCh38 4 158,695,294
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001281738.1:c.502-203A>G
NM_001281737.2:c.544-203A>G
NM_004453.4:c.685-203A>G
NG_007078.2:g.27953A>G
More... 		06/28/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ETFDH
Accession:NM_001281738
Location:INTRON

Gene Symbol:ETFDH
Accession:NM_004453
Location:INTRON

Gene Symbol:ETFDH
Accession:NM_001281737
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001567020 CLINVAR
dbSNP (RS) rs146221617 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ETFDH CLINVAR
OMIM 231675 CLINVAR